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Metabolic profiling for dissection of late leaf spot disease resistance mechanism in groundnut
Late leaf spot (LLS) caused by fungi Passalora personata is generally more destructive and difficult to control than early leaf spot. The aim of this study was to decipher biochemical defense mechanism in groundnut genotypes against P. personata by identifying resistance specific biomarkers and meta...
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Published in: | Physiology and molecular biology of plants 2021-05, Vol.27 (5), p.1027-1041 |
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creator | Mahatma, M. K. Thawait, Lokesh Kumar Jadon, K. S. Thirumalaisamy, P. P. Bishi, S. K. Rathod, Khyati J. Verma, Aman Kumar, Narendra Golakiya, B. A. |
description | Late leaf spot (LLS) caused by fungi
Passalora personata
is generally more destructive and difficult to control than early leaf spot. The aim of this study was to decipher biochemical defense mechanism in groundnut genotypes against
P. personata
by identifying resistance specific biomarkers and metabolic pathways induced during host–pathogen interaction. Metabolomics of non-infected and infected leaves of moderately resistant (GPBD4 and ICGV86590), resistant (KDG128 and RHRG06083) and susceptible (GG20, JL24 and TMV2) genotypes was carried out at 5 days after infection (65 days after sowing). Non-targeted metabolite analysis using GC–MS revealed total 77 metabolites including carbohydrates, sugar alcohols, amino acids, fatty acids, polyamines, phenolics, terpenes and sterols. Variable importance in projection (VIP) measure of partial least squares-discriminant analysis (PLS-DA) showed that resistant and moderately resistant genotypes possessed higher intensities of ribonic acid, cinnamic acid, malic acid, squalene, xylulose, galactose, fructose, glucose, β-amyrin and hydroquinone while susceptible genotypes had higher amount of gluconic acid 2-methoxime, ribo-hexose-3-ulose and gluconic acid. Heat map analysis showed that resistant genotypes had higher intensities of β-amyrin, hydroquinone in non-infected and malic acid, squalene, putrescine and 2,3,4-trihydroxybutyric acid in infected leaves. Dendrogram analysis further separated resistant genotypes in the same cluster along with infected moderately resistant genotypes. The most significant pathways identified are: linoleic acid metabolism, flavone and flavonol biosynthesis, cutin, suberin and wax biosynthesis, pentose and glucuronate interconversions, starch and sucrose metabolism, stilbenoid biosynthesis and ascorbate and aldarate metabolism. Targeted metabolite analysis further confirmed that resistant genotypes possessed higher content of primary metabolites sucrose, glucose, fructose, malic acid and citric acid. Moreover, resistant genotypes possessed higher content of salicylic, coumaric, ferulic, cinnamic, gallic acid (phenolic acids) and kaempferol, quercetin and catechin (flavonols). Thus metabolites having higher accumulation in resistant genotypes can be used as biomarkers for screening of LSS resistant germplasm. These results unravel that higher amount of primary metabolites leads to stimulate the accumulation of more amounts of secondary metabolites such as phenolic acid, flavanols, stilbene |
doi_str_mv | 10.1007/s12298-021-00985-5 |
format | article |
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Passalora personata
is generally more destructive and difficult to control than early leaf spot. The aim of this study was to decipher biochemical defense mechanism in groundnut genotypes against
P. personata
by identifying resistance specific biomarkers and metabolic pathways induced during host–pathogen interaction. Metabolomics of non-infected and infected leaves of moderately resistant (GPBD4 and ICGV86590), resistant (KDG128 and RHRG06083) and susceptible (GG20, JL24 and TMV2) genotypes was carried out at 5 days after infection (65 days after sowing). Non-targeted metabolite analysis using GC–MS revealed total 77 metabolites including carbohydrates, sugar alcohols, amino acids, fatty acids, polyamines, phenolics, terpenes and sterols. Variable importance in projection (VIP) measure of partial least squares-discriminant analysis (PLS-DA) showed that resistant and moderately resistant genotypes possessed higher intensities of ribonic acid, cinnamic acid, malic acid, squalene, xylulose, galactose, fructose, glucose, β-amyrin and hydroquinone while susceptible genotypes had higher amount of gluconic acid 2-methoxime, ribo-hexose-3-ulose and gluconic acid. Heat map analysis showed that resistant genotypes had higher intensities of β-amyrin, hydroquinone in non-infected and malic acid, squalene, putrescine and 2,3,4-trihydroxybutyric acid in infected leaves. Dendrogram analysis further separated resistant genotypes in the same cluster along with infected moderately resistant genotypes. The most significant pathways identified are: linoleic acid metabolism, flavone and flavonol biosynthesis, cutin, suberin and wax biosynthesis, pentose and glucuronate interconversions, starch and sucrose metabolism, stilbenoid biosynthesis and ascorbate and aldarate metabolism. Targeted metabolite analysis further confirmed that resistant genotypes possessed higher content of primary metabolites sucrose, glucose, fructose, malic acid and citric acid. Moreover, resistant genotypes possessed higher content of salicylic, coumaric, ferulic, cinnamic, gallic acid (phenolic acids) and kaempferol, quercetin and catechin (flavonols). Thus metabolites having higher accumulation in resistant genotypes can be used as biomarkers for screening of LSS resistant germplasm. These results unravel that higher amount of primary metabolites leads to stimulate the accumulation of more amounts of secondary metabolites such as phenolic acid, flavanols, stilbenes and terpenoids (squalene and β-amyrin) biosynthesis which are ultimately involved in defense mechanism against LLS pathogen.</description><identifier>ISSN: 0971-5894</identifier><identifier>EISSN: 0974-0430</identifier><identifier>DOI: 10.1007/s12298-021-00985-5</identifier><identifier>PMID: 34108825</identifier><language>eng</language><publisher>New Delhi: Springer India</publisher><subject>Accumulation ; Acid resistance ; Alcohols ; Amino acids ; Ascorbic acid ; Biological and Medical Physics ; Biomarkers ; Biomedical and Life Sciences ; Biophysics ; Biosynthesis ; Carbohydrates ; Catechin ; Cell Biology ; Cinnamic acid ; Citric acid ; Cutin ; Defense mechanisms ; Discriminant analysis ; Disease resistance ; Fatty acids ; Flavanols ; Flavonols ; Fructose ; Galactose ; Gallic acid ; Genotypes ; Germplasm ; Gluconic acid ; Glucose ; Groundnuts ; Hexose ; Hydroquinone ; Leafspot ; Leaves ; Life Sciences ; Malic acid ; Metabolism ; Metabolites ; Pathogens ; Phenols ; Plant Physiology ; Plant Sciences ; Polyamines ; Research Article ; Secondary metabolites ; Terpenes</subject><ispartof>Physiology and molecular biology of plants, 2021-05, Vol.27 (5), p.1027-1041</ispartof><rights>Prof. H.S. Srivastava Foundation for Science and Society 2021</rights><rights>Prof. H.S. Srivastava Foundation for Science and Society 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-79fdc57c4cdec540d47fcb29ee1eb7363cca6bf982ad20192e0679c4e2cec1193</citedby><cites>FETCH-LOGICAL-c474t-79fdc57c4cdec540d47fcb29ee1eb7363cca6bf982ad20192e0679c4e2cec1193</cites><orcidid>0000-0002-9596-0076</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140181/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140181/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34108825$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mahatma, M. K.</creatorcontrib><creatorcontrib>Thawait, Lokesh Kumar</creatorcontrib><creatorcontrib>Jadon, K. S.</creatorcontrib><creatorcontrib>Thirumalaisamy, P. P.</creatorcontrib><creatorcontrib>Bishi, S. K.</creatorcontrib><creatorcontrib>Rathod, Khyati J.</creatorcontrib><creatorcontrib>Verma, Aman</creatorcontrib><creatorcontrib>Kumar, Narendra</creatorcontrib><creatorcontrib>Golakiya, B. A.</creatorcontrib><title>Metabolic profiling for dissection of late leaf spot disease resistance mechanism in groundnut</title><title>Physiology and molecular biology of plants</title><addtitle>Physiol Mol Biol Plants</addtitle><addtitle>Physiol Mol Biol Plants</addtitle><description>Late leaf spot (LLS) caused by fungi
Passalora personata
is generally more destructive and difficult to control than early leaf spot. The aim of this study was to decipher biochemical defense mechanism in groundnut genotypes against
P. personata
by identifying resistance specific biomarkers and metabolic pathways induced during host–pathogen interaction. Metabolomics of non-infected and infected leaves of moderately resistant (GPBD4 and ICGV86590), resistant (KDG128 and RHRG06083) and susceptible (GG20, JL24 and TMV2) genotypes was carried out at 5 days after infection (65 days after sowing). Non-targeted metabolite analysis using GC–MS revealed total 77 metabolites including carbohydrates, sugar alcohols, amino acids, fatty acids, polyamines, phenolics, terpenes and sterols. Variable importance in projection (VIP) measure of partial least squares-discriminant analysis (PLS-DA) showed that resistant and moderately resistant genotypes possessed higher intensities of ribonic acid, cinnamic acid, malic acid, squalene, xylulose, galactose, fructose, glucose, β-amyrin and hydroquinone while susceptible genotypes had higher amount of gluconic acid 2-methoxime, ribo-hexose-3-ulose and gluconic acid. Heat map analysis showed that resistant genotypes had higher intensities of β-amyrin, hydroquinone in non-infected and malic acid, squalene, putrescine and 2,3,4-trihydroxybutyric acid in infected leaves. Dendrogram analysis further separated resistant genotypes in the same cluster along with infected moderately resistant genotypes. The most significant pathways identified are: linoleic acid metabolism, flavone and flavonol biosynthesis, cutin, suberin and wax biosynthesis, pentose and glucuronate interconversions, starch and sucrose metabolism, stilbenoid biosynthesis and ascorbate and aldarate metabolism. Targeted metabolite analysis further confirmed that resistant genotypes possessed higher content of primary metabolites sucrose, glucose, fructose, malic acid and citric acid. Moreover, resistant genotypes possessed higher content of salicylic, coumaric, ferulic, cinnamic, gallic acid (phenolic acids) and kaempferol, quercetin and catechin (flavonols). Thus metabolites having higher accumulation in resistant genotypes can be used as biomarkers for screening of LSS resistant germplasm. These results unravel that higher amount of primary metabolites leads to stimulate the accumulation of more amounts of secondary metabolites such as phenolic acid, flavanols, stilbenes and terpenoids (squalene and β-amyrin) biosynthesis which are ultimately involved in defense mechanism against LLS pathogen.</description><subject>Accumulation</subject><subject>Acid resistance</subject><subject>Alcohols</subject><subject>Amino acids</subject><subject>Ascorbic acid</subject><subject>Biological and Medical Physics</subject><subject>Biomarkers</subject><subject>Biomedical and Life Sciences</subject><subject>Biophysics</subject><subject>Biosynthesis</subject><subject>Carbohydrates</subject><subject>Catechin</subject><subject>Cell Biology</subject><subject>Cinnamic acid</subject><subject>Citric acid</subject><subject>Cutin</subject><subject>Defense mechanisms</subject><subject>Discriminant analysis</subject><subject>Disease resistance</subject><subject>Fatty acids</subject><subject>Flavanols</subject><subject>Flavonols</subject><subject>Fructose</subject><subject>Galactose</subject><subject>Gallic acid</subject><subject>Genotypes</subject><subject>Germplasm</subject><subject>Gluconic acid</subject><subject>Glucose</subject><subject>Groundnuts</subject><subject>Hexose</subject><subject>Hydroquinone</subject><subject>Leafspot</subject><subject>Leaves</subject><subject>Life Sciences</subject><subject>Malic acid</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Pathogens</subject><subject>Phenols</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Polyamines</subject><subject>Research Article</subject><subject>Secondary metabolites</subject><subject>Terpenes</subject><issn>0971-5894</issn><issn>0974-0430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kU1rFTEUhoMotlb_gAsJuHEzevIxk2QjSPELKm50a8hkTm5TZpJrkin4753bW-vHwlUC73Pe5PAQ8pTBSwagXlXGudEdcNYBGN13_T1yCkbJDqSA-zd31vXayBPyqNYrgEFIxR6SEyEZaM37U_LtEzY35jl6ui85xDmmHQ250CnWir7FnGgOdHYN6Ywu0LrP7RCiq0gL1libSx7pgv7SpVgXGhPdlbymKa3tMXkQ3Fzxye15Rr6-e_vl_EN38fn9x_M3F52XSrZOmTD5XnnpJ_S9hEmq4EduEBmOSgzCezeMwWjuJg7McIRBGS-Re_SMGXFGXh979-u44OQxteJmuy9xceWHzS7av5MUL-0uX1vNJDDNtoIXtwUlf1-xNrvE6nGeXcK8Vst7YbQexCA39Pk_6FVeS9rWO1AgueagNoofKV9yrQXD3WcY2IM-e9RnN332Rp_tt6Fnf65xN_LL1waII1C3KO2w_H77P7U_ARY9qEo</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Mahatma, M. K.</creator><creator>Thawait, Lokesh Kumar</creator><creator>Jadon, K. S.</creator><creator>Thirumalaisamy, P. P.</creator><creator>Bishi, S. K.</creator><creator>Rathod, Khyati J.</creator><creator>Verma, Aman</creator><creator>Kumar, Narendra</creator><creator>Golakiya, B. A.</creator><general>Springer India</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9596-0076</orcidid></search><sort><creationdate>20210501</creationdate><title>Metabolic profiling for dissection of late leaf spot disease resistance mechanism in groundnut</title><author>Mahatma, M. K. ; Thawait, Lokesh Kumar ; Jadon, K. S. ; Thirumalaisamy, P. P. ; Bishi, S. K. ; Rathod, Khyati J. ; Verma, Aman ; Kumar, Narendra ; Golakiya, B. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-79fdc57c4cdec540d47fcb29ee1eb7363cca6bf982ad20192e0679c4e2cec1193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Accumulation</topic><topic>Acid resistance</topic><topic>Alcohols</topic><topic>Amino acids</topic><topic>Ascorbic acid</topic><topic>Biological and Medical Physics</topic><topic>Biomarkers</topic><topic>Biomedical and Life Sciences</topic><topic>Biophysics</topic><topic>Biosynthesis</topic><topic>Carbohydrates</topic><topic>Catechin</topic><topic>Cell Biology</topic><topic>Cinnamic acid</topic><topic>Citric acid</topic><topic>Cutin</topic><topic>Defense mechanisms</topic><topic>Discriminant analysis</topic><topic>Disease resistance</topic><topic>Fatty acids</topic><topic>Flavanols</topic><topic>Flavonols</topic><topic>Fructose</topic><topic>Galactose</topic><topic>Gallic acid</topic><topic>Genotypes</topic><topic>Germplasm</topic><topic>Gluconic acid</topic><topic>Glucose</topic><topic>Groundnuts</topic><topic>Hexose</topic><topic>Hydroquinone</topic><topic>Leafspot</topic><topic>Leaves</topic><topic>Life Sciences</topic><topic>Malic acid</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Pathogens</topic><topic>Phenols</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Polyamines</topic><topic>Research Article</topic><topic>Secondary metabolites</topic><topic>Terpenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mahatma, M. K.</creatorcontrib><creatorcontrib>Thawait, Lokesh Kumar</creatorcontrib><creatorcontrib>Jadon, K. S.</creatorcontrib><creatorcontrib>Thirumalaisamy, P. P.</creatorcontrib><creatorcontrib>Bishi, S. K.</creatorcontrib><creatorcontrib>Rathod, Khyati J.</creatorcontrib><creatorcontrib>Verma, Aman</creatorcontrib><creatorcontrib>Kumar, Narendra</creatorcontrib><creatorcontrib>Golakiya, B. A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Physiology and molecular biology of plants</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mahatma, M. K.</au><au>Thawait, Lokesh Kumar</au><au>Jadon, K. S.</au><au>Thirumalaisamy, P. P.</au><au>Bishi, S. K.</au><au>Rathod, Khyati J.</au><au>Verma, Aman</au><au>Kumar, Narendra</au><au>Golakiya, B. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic profiling for dissection of late leaf spot disease resistance mechanism in groundnut</atitle><jtitle>Physiology and molecular biology of plants</jtitle><stitle>Physiol Mol Biol Plants</stitle><addtitle>Physiol Mol Biol Plants</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>27</volume><issue>5</issue><spage>1027</spage><epage>1041</epage><pages>1027-1041</pages><issn>0971-5894</issn><eissn>0974-0430</eissn><abstract>Late leaf spot (LLS) caused by fungi
Passalora personata
is generally more destructive and difficult to control than early leaf spot. The aim of this study was to decipher biochemical defense mechanism in groundnut genotypes against
P. personata
by identifying resistance specific biomarkers and metabolic pathways induced during host–pathogen interaction. Metabolomics of non-infected and infected leaves of moderately resistant (GPBD4 and ICGV86590), resistant (KDG128 and RHRG06083) and susceptible (GG20, JL24 and TMV2) genotypes was carried out at 5 days after infection (65 days after sowing). Non-targeted metabolite analysis using GC–MS revealed total 77 metabolites including carbohydrates, sugar alcohols, amino acids, fatty acids, polyamines, phenolics, terpenes and sterols. Variable importance in projection (VIP) measure of partial least squares-discriminant analysis (PLS-DA) showed that resistant and moderately resistant genotypes possessed higher intensities of ribonic acid, cinnamic acid, malic acid, squalene, xylulose, galactose, fructose, glucose, β-amyrin and hydroquinone while susceptible genotypes had higher amount of gluconic acid 2-methoxime, ribo-hexose-3-ulose and gluconic acid. Heat map analysis showed that resistant genotypes had higher intensities of β-amyrin, hydroquinone in non-infected and malic acid, squalene, putrescine and 2,3,4-trihydroxybutyric acid in infected leaves. Dendrogram analysis further separated resistant genotypes in the same cluster along with infected moderately resistant genotypes. The most significant pathways identified are: linoleic acid metabolism, flavone and flavonol biosynthesis, cutin, suberin and wax biosynthesis, pentose and glucuronate interconversions, starch and sucrose metabolism, stilbenoid biosynthesis and ascorbate and aldarate metabolism. Targeted metabolite analysis further confirmed that resistant genotypes possessed higher content of primary metabolites sucrose, glucose, fructose, malic acid and citric acid. Moreover, resistant genotypes possessed higher content of salicylic, coumaric, ferulic, cinnamic, gallic acid (phenolic acids) and kaempferol, quercetin and catechin (flavonols). Thus metabolites having higher accumulation in resistant genotypes can be used as biomarkers for screening of LSS resistant germplasm. These results unravel that higher amount of primary metabolites leads to stimulate the accumulation of more amounts of secondary metabolites such as phenolic acid, flavanols, stilbenes and terpenoids (squalene and β-amyrin) biosynthesis which are ultimately involved in defense mechanism against LLS pathogen.</abstract><cop>New Delhi</cop><pub>Springer India</pub><pmid>34108825</pmid><doi>10.1007/s12298-021-00985-5</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-9596-0076</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Accumulation Acid resistance Alcohols Amino acids Ascorbic acid Biological and Medical Physics Biomarkers Biomedical and Life Sciences Biophysics Biosynthesis Carbohydrates Catechin Cell Biology Cinnamic acid Citric acid Cutin Defense mechanisms Discriminant analysis Disease resistance Fatty acids Flavanols Flavonols Fructose Galactose Gallic acid Genotypes Germplasm Gluconic acid Glucose Groundnuts Hexose Hydroquinone Leafspot Leaves Life Sciences Malic acid Metabolism Metabolites Pathogens Phenols Plant Physiology Plant Sciences Polyamines Research Article Secondary metabolites Terpenes |
title | Metabolic profiling for dissection of late leaf spot disease resistance mechanism in groundnut |
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